DISEASES

Disease-gene associations mined from literature

Human genes for xeroderma pigmentosum group G

Xeroderma pigmentosum group G [DOID:0110849]

A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33.

Synonyms:  xeroderma pigmentosum group G,  DOID:0110849,  xeroderma pigmentosum group Gs,  XP group G,  XP7 ...